A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527351



Internal ID15107958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:96907772..96914050hg38UCSC Ensembl
Innerchr10:98667529..98673807hg19UCSC Ensembl
Innerchr10:98657519..98663797hg18UCSC Ensembl
Innerchr10:98657519..98663797hg17UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg386279
hg196279
hg186279
hg176279
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703780
Samples
Known GenesLCOR
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527351
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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